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anti-Human Adiponectin Receptor 1 Antibodies:
anti-Mouse (Murine) Adiponectin Receptor 1 Antibodies:
anti-Rat (Rattus) Adiponectin Receptor 1 Antibodies:
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Human Polyclonal Adiponectin Receptor 1 Primary Antibody for IF (p), IHC (p) - ABIN670836
Liu, Wu, Zhang, Chen, Liu, Wu, Zhu: The ameliorating effect of rosiglitazone on experimental nonalcoholic steatohepatitis is associated with regulating adiponectin receptor expression in rats. in European journal of pharmacology 2010
Show all 10 Pubmed References
Human Polyclonal Adiponectin Receptor 1 Primary Antibody for IHC (p), IHC - ABIN440478
Staiger, Kaltenbach, Staiger, Stefan, Fritsche, Guirguis, Péterfi, Weisser, Machicao, Stumvoll, Häring: Expression of adiponectin receptor mRNA in human skeletal muscle cells is related to in vivo parameters of glucose and lipid metabolism. in Diabetes 2004
Show all 6 Pubmed References
Chicken Polyclonal Adiponectin Receptor 1 Primary Antibody for IHC, ELISA - ABIN1585580
Duivenvoorden, Paschos, Hopmans, Austin, Pinthus: Endoplasmic reticulum protein ERp46 in renal cell carcinoma. in PLoS ONE 2014
Human Polyclonal Adiponectin Receptor 1 Primary Antibody for IHC, WB - ABIN1169254
Corbetta, Redaelli, Pozzi, Bovo, Ratti, Redaelli, Pellegrini, Beck-Peccoz, Spada: Fibrosis is associated with adiponectin resistance in chronic hepatitis C virus infection. in European journal of clinical investigation 2011
Broad Bean (Vicia faba) Polyclonal Adiponectin Receptor 1 Primary Antibody for IHC (p) - ABIN2477287
Shen, Li, Li, Wu, Ding: Pioglitazone prevents hyperglycemia induced decrease of AdipoR1 and AdipoR2 in coronary arteries and coronary VSMCs. in Molecular and cellular endocrinology 2012
Adiponectin and adiponectin receptor genes are coexpressed during zebrafish embryogenesis and regulated by food deprivation
Renoprotection of adiponectin is associated with improvement of the endothelial dysfunction, reduction of oxidative stress, and upregulation of endothelial nitric oxide synthase (show NOS3 Antibodies) expression through activation of adenosine 5'-monophosphate-activated protein kinase (show CDK7 Antibodies) by AdipoR1 and activation of peroxisome proliferator-activated receptor (show PPARD Antibodies) (PPAR)-alpha (show PPARA Antibodies) signaling pathway by AdipoR2 (show ADIPOR2 Antibodies). [review]
High ADIPOR1 expression is associated with breast cancer.
revised ADIPOR1 crystal structure exhibiting a seven-transmembrane-domain architecture that is clearly distinct from that of ADIPOR2 (show ADIPOR2 Antibodies)
TNF-alpha (show TNF Antibodies) impairs adiponectin/AdipoR1 signaling, mitochondrial biogenesis, and myogenesis in primary human myotubes cultures obtained from heart failure patients.
the knockdown phenotype was partially rescued by injecting wild-type, but not mutant, human ADIPOR1 mRNA. We conclude that ADIPOR1 is a novel adRP (show PLIN2 Antibodies)-causing gene and plays an important role in rod development and maintenance.
Adiponectin stimulates cPLA2 and COX-2 expression via AdipoR1/2-dependent activation of PKC/NADPH oxidase/mitochondria resulting in ROS accumulation, p300 phosphorylation, and histone H4 acetylation.
Decreased expression of ADIPOR1 is associated with polycystic ovary syndrome.
sequence- and structure-based computational tools were employed in this study to functionally and structurally characterize the coding Nonsynonymous Single Nucleotide Polymorphisms of ADIPOR1 gene listed in the single nucleotide polymorphisms database.
PCR results showed expression of adiponectin, AdipoR1, AdipoR2 (show ADIPOR2 Antibodies), follicle-stimulating hormone receptor (FSHR (show FSHR Antibodies)), and luteinizing hormone receptor (LHR (show LHCGR Antibodies)) in granulosa cells (GCs (show GCLC Antibodies)). After controlling body mass index (BMI) values, qRT-PCR demonstrated a decreased expression of adiponectin system in GCs (show GCLC Antibodies) of polycystic ovary syndromepatients compared to those in controls
ADPOR1 variants, rs3737884*G and rs7514221*C, may be shared risk factors associated with CAD (show CAD Antibodies), T2D, and T2D with CAD (show CAD Antibodies) in a population of northeast China.
Immunofluorescence indicated that GPRC6A (show GPRC6A Antibodies) and adiponectin receptor 1 were co-localized in mouse muscle tissues. The present finding suggested adiponectin receptor 1 can mediate the improvement of glucose metabolism by osteocalcin (show BGLAP Antibodies) in ovariectomized mice
adiponectin maintains intestinal homeostasis and protects against murine colitis through interactions with its receptor AdipoR1 and by modulating adaptive immunity and STAT3 (show STAT3 Antibodies) signaling
Based on these findings, this study showed that CTRP9 (show C1QTNF9 Antibodies) might induce mitochondrial biogenesis and protect high glucose-induced endothelial oxidative damage via AdipoR1-SIRT1 (show SIRT1 Antibodies)-PGC-1alpha (show PPARGC1A Antibodies) signaling pathway.
High salt is an important suppressor of cardioprotective APN (show ANPEP Antibodies) and AdipoR1 in cardiac myocytes.
AdipoR1, not AdipoR2 (show ADIPOR2 Antibodies), was first identified as a receptor of CTRP6 during the process of mitotic clonal expansion. Collectively, we suggest that CTRP6 mediates the ectopic lipogenesis through AdipoR1/Erk (show EPHB2 Antibodies)/PPARgamma (show PPARG Antibodies) signaling pathway in myoblasts.
The results demonstrated a dynamic dysfunction of APN (show ANPEP Antibodies)/AdipoR1 axis accompanying progression of diabetes mellitus in mice with cerebral ischemia.
physiologic adiponectin levels enhance the vasorelaxative response to acetylcholine by inducing nitric oxide production through AdipoR1/Cav-1 (show CAV1 Antibodies) mediated signaling.
AdipoR1 is expressed on adipose tissue-resident Tregs, mainly Helios (show ZNFN1A2 Antibodies)(+) Tregs, and this expression is dependent on weight and fat accumulation. This data proposes a new mechanism through which weight gain might alter immunoregulation.
Adiponectin directly acts on murine dermal gammadelta-T cells to suppress IL-17 (show IL17A Antibodies) synthesis via AdipoR1.
At high glucose concentrations in vitro, AdipoR1 regulated the survival of neural stem cells through the p53 (show TP53 Antibodies)/p21 (show D4S234E Antibodies) pathway and the proliferation- and differentiation-related factors of neural stem cells via TLX (show NR2E1 Antibodies).
This study demonstrated the presence of adiponectin and its receptors in the uteri, conceptuses, and trophoblasts of pregnant pigs and that the local adiponectin system is dependent on the stage of pregnancy.
Data suggest AdipoR1/adiponectin signaling up-regulates gene expression of hepatocyte enzymes involved in fatty acid metabolism and protects hepatocyte from nonesterified fatty acids by activating phosphatidylinositol 3-kinase (PI3K/AKT (show AKT1 Antibodies)) signaling.
study demonstrated that adiponectin and adiponectin receptors 1 and 2 messenger RNAs and proteins are present in the porcine hypothalamus and that their expression levels are determined by the pig's endocrine status related to the oestrous cycle
This study demonstrated the presence of adiponectin, AdipoR1 and AdipoR2 genes and proteins in the porcine uterus and the effect of the stage of the oestrous cycle on the expression of the adiponectin system.
Data indicate that AdipoR1 and AdipoR2 mRNAs and proteins are present in the porcine pituitary and that adiponectin receptors expression is dependent on endocrine status of the animals.
Results showed a high polymorphism of the ADIPOR1 and a complexity in its transcription level in longissimus dorsi from five pig breeds: Duroc, Polish Large White, Polish Landrace, Pietrain and Pulawska.
The cloning and characterization of adiponectin, ADIPOR1, and ADIPOR2 (show ADIPOR2 Antibodies) are reported.
FISH localization of 4 BAC clones harbouring potential candidate genes for fatness traits: DGAT1 (show DGAT1 Antibodies) (SSC4p15), PPARA (show PPARA Antibodies) (SSC5p15), ADIPOR1 (SSC10p13) and CREB (show CREB1 Antibodies) (SSC15q24)
Insulin regulates the expression of adiponectin and adiponectin receptors in porcine adipocytes.
Low level expression of adiponectin mRNA was found in all areas of bovine mammary gland tissues examined. AdipoR1 and AdipoR2 (show ADIPOR2 Antibodies) mRNAs were also detected in mammary tissues and their expression was particularly prominent in the parenchyma and cistern.
The physiologic status of the ovary has significant effects on the natural expression patterns of adiponectin and its receptors in follicular and luteal cells of bovine ovary.
This gene encodes a protein which acts as a receptor for adiponectin, a hormone secreted by adipocytes which regulates fatty acid catabolism and glucose levels. Binding of adiponectin to the encoded protein results in activation of an AMP-activated kinase signaling pathway which affects levels of fatty acid oxidation and insulin sensitivity. A pseudogene of this gene is located on chromosome 14.
adiponectin receptor 1
, adiponectin receptor type I
, adiponectin receptor protein 1
, progestin and adipoQ receptor family member I
, adiponectin receptor protein 1-like